At a Glance
- Tasks: Lead clinical programming activities, ensuring quality and efficiency in data management.
- Company: Join Johnson & Johnson, a leader in healthcare innovation dedicated to improving global health.
- Benefits: Enjoy hybrid work options, a diverse culture, and opportunities for personal growth.
- Why this job: Make a real impact on healthcare while working with cutting-edge technology and a supportive team.
- Qualifications: Bachelor's degree in a relevant field and 6-8 years of clinical programming experience required.
- Other info: Embrace a culture of inclusion and belonging at a company committed to diversity.
The predicted salary is between 48000 - 72000 £ per year.
Johnson & Johnson are currently seeking a Clinical Programming Lead, Clinical Programming to join our Integrated Data Analytics & Reporting (IDAR) Department. This position is based in High Wycombe (Hybrid). Remote work options in the UK may be considered on a case-by-case basis and if approved by the company.
The Clinical Programming Lead is an experienced clinical trial programmer with expertise in industry standard and complex data structures, programming languages, and/or reporting solutions with proven technical capabilities in leading clinical trial activities and/or teams in accordance with departmental processes and procedures. The position is responsible for providing expertise, planning, creation and oversight of one or more clinical programming trial activities of moderate to high complexity/criticality, including data models for fit for purpose reporting consumption and/or CDISC submission ready SDTM tabulation packages (aCRF, define.xml, cSDRG, etc). Creates and executes edit check programs, cross and study specific reporting solutions to aid in monitoring of safety, risk, compliance and ensures quality data review. Responsible for creating efficiencies in the clinical data flow using metadata driven approaches and ensuring the highest level of consistency and quality across trials they support.
Role and Responsibilities
- Accountable for one or more clinical programming trial activities of moderate to high complexity, scope and/or criticality.
- Performs comprehensive review of, and provides input into, project requirements and documentation.
- Identifies gaps, proposes solutions and applies expertise to improve efficiency of programming tasks and/or improve overall quality of programming deliverables.
- Provides technical and project specific guidance to team members to ensure high quality and on-time deliverables in compliance with departmental processes.
- Ensures latest standards are being utilized, current technologies are deployed.
- Responsible for planning, coordination, oversight and execution of team activities as appropriate and provides technical and project specific guidance to team members to ensure quality and on-time deliverables in compliance with departmental processes and procedures.
- Create and/or review specifications for mapping internal data review model for fit for purpose reporting consumption and/or submission ready CDISC SDTM.
- Design mapping algorithms for nonstandard conversions.
- Responsible for creation or review of internal data model fit for purpose reporting consumption and/or submission ready CDISC SDTM packages for health authority submissions and keeping abreast in changing regulatory requirements.
- Program, or oversight of quality review checks, cross and study specific reports for use by team members and consumers of data.
Qualifications
- Bachelor’s degree or higher and/or equivalent in computer science, data science/data engineering, mathematics or another relevant scientific field (or equivalent theoretical/technical depth).
- Approximately 6-8+ years of clinical programming/clinical data management experience with increasing responsibility, preferably in the pharmaceutical/clinical trial environment.
- In-depth knowledge of data structures and relevant programming languages for data manipulation and reporting. May include SAS, R, Python, etc. Knowledge of SAS is required.
- Advanced CDISC SDTM knowledge.
- Experience in planning and coordinating one or more team activities as necessary.
- Demonstrated written and verbal communications skills.
- Working knowledge of regulatory guidelines (e.g. ICH-GCP) and relevant clinical R&D concepts.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges. We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential. At Johnson & Johnson, we all belong.
Primary Location: Europe/Middle East/Africa-United Kingdom-England-High Wycombe
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our page for information on how to request an accommodation.
Sr Clin Prog Lead employer: Johnson & Johnson
Contact Detail:
Johnson & Johnson Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Sr Clin Prog Lead
✨Tip Number 1
Familiarise yourself with the latest CDISC SDTM standards and regulatory guidelines. This knowledge will not only help you understand the requirements of the role but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals in the clinical programming field, especially those who have experience at Johnson & Johnson or similar companies. Engaging with them can provide insights into the company culture and expectations for the role.
✨Tip Number 3
Prepare to discuss specific examples of how you've improved efficiency in clinical programming tasks in your previous roles. Highlighting your problem-solving skills and ability to lead projects will set you apart from other candidates.
✨Tip Number 4
Showcase your technical skills in programming languages like SAS, R, or Python during any interviews or discussions. Being able to articulate your experience with these tools will be crucial in demonstrating your fit for the position.
We think you need these skills to ace Sr Clin Prog Lead
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical programming and data management. Emphasise your expertise with programming languages like SAS, R, or Python, and any specific projects that align with the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: Write a cover letter that connects your background to the role of Clinical Programming Lead. Discuss your experience in leading clinical trial activities and how you can contribute to Johnson & Johnson's mission of healthcare innovation.
Highlight Technical Skills: Clearly list your technical skills related to data structures and programming languages. Mention your advanced knowledge of CDISC SDTM and any experience with regulatory guidelines, as these are crucial for the position.
Showcase Communication Abilities: Since the role requires strong written and verbal communication skills, provide examples of how you've effectively communicated complex information in previous roles. This could include leading team meetings or presenting project updates.
How to prepare for a job interview at Johnson & Johnson
✨Showcase Your Technical Expertise
As a Clinical Programming Lead, you'll need to demonstrate your proficiency in programming languages like SAS, R, or Python. Be prepared to discuss specific projects where you've applied these skills, particularly in clinical trial settings.
✨Understand Regulatory Guidelines
Familiarise yourself with regulatory guidelines such as ICH-GCP and CDISC standards. During the interview, highlight your experience in ensuring compliance with these regulations in your previous roles.
✨Demonstrate Leadership Skills
Since this role involves leading teams, be ready to share examples of how you've successfully coordinated team activities and provided guidance to colleagues. Discuss any challenges you faced and how you overcame them.
✨Prepare for Problem-Solving Questions
Expect questions that assess your ability to identify gaps in project requirements and propose solutions. Think of specific instances where you've improved efficiency or quality in programming tasks and be ready to discuss them.